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Radiation
UroLift + SAbR for Prostate Cancer
Phase 1
Recruiting
Led By Aurelie Garant, MD
Research Sponsored by University of Texas Southwestern Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Eastern Cooperative Oncology Group (ECOG) Performance status 0-1.
Age > 45 years.
Must not have
Prior pelvic radiotherapy, chemotherapy, or surgery for prostate cancer.
Urethral conditions (e.g. urethral strictures and neoplams) that may prevent insertion of UroLift System delivery system into the bladder
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 90 days
Awards & highlights
No Placebo-Only Group
Summary
This trial combines the UroLift System, which helps men with an enlarged prostate by opening up the urinary passage, with a precise radiation treatment for prostate cancer. It targets men who have both conditions to improve their treatment outcomes. The UroLift System is a minimally invasive treatment designed to improve lower urinary tract symptoms in men with an enlarged prostate without affecting sexual function.
Who is the study for?
Men over 45 with early-stage prostate cancer and BPH, ECOG status 0-1, ASA score of 1-3. PSA <20 ng/ml, willing to use contraception. No prior prostate treatments or active infections; no urinary incontinence or conditions preventing UroLift insertion.
What is being tested?
The trial tests the safety of using the UroLift System before Stereotactic Ablative Radiotherapy (SAbR) in men with newly diagnosed prostate cancer who also have BPH by monitoring complications within 90 days post-treatment.
What are the potential side effects?
Potential side effects may include discomfort from UroLift implantation, typical risks associated with general anesthesia, and common radiotherapy side effects like fatigue, skin reactions, and urinary issues.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am fully active or can carry out light work.
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I am older than 45 years.
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My urinary symptoms are severe, with an AUA score of 17 or more.
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My prostate cancer is early stage, not spread, with specific Gleason scores.
Select...
My prostate is smaller than 100 grams, as measured by ultrasound or MRI.
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My health is good to moderately impaired.
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I can be safely put under general anesthesia for less than an hour.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have had treatments like radiotherapy, chemotherapy, or surgery for prostate cancer.
Select...
I don't have urethral conditions that would prevent UroLift System procedures.
Select...
I am currently on hormone therapy for cancer.
Select...
I have urinary incontinence because of a weak bladder sphincter.
Select...
I currently have a urinary tract infection.
Select...
I have had surgery or procedures for an enlarged prostate.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 90 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~90 days
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Safety of UroLift implant when combined with SAbR for men with prostate cancer and benign prostatic hyperplasia
Secondary study objectives
Quality of Life with UroLift System
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: All Study participantsExperimental Treatment2 Interventions
Study participants will undergo Urolift System followed by SABR
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
SABR
2012
Completed Phase 2
~110
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The UroLift System mechanically lifts and holds the enlarged prostate tissue, relieving urinary obstruction without cutting, heating, or removing tissue, offering a minimally invasive option with fewer side effects. Other common treatments include radical prostatectomy (surgical removal of the prostate gland), radiation therapy (high-energy rays to kill cancer cells), and hormone therapy (reducing or blocking testosterone production).
These treatments are essential for managing or eradicating cancer while preserving the patient's quality of life by minimizing adverse effects.
Find a Location
Who is running the clinical trial?
University of Texas Southwestern Medical CenterLead Sponsor
1,080 Previous Clinical Trials
1,056,298 Total Patients Enrolled
16 Trials studying Prostate Cancer
2,145 Patients Enrolled for Prostate Cancer
NeoTract, Inc.Industry Sponsor
10 Previous Clinical Trials
3,385 Total Patients Enrolled
Aurelie Garant, MDPrincipal InvestigatorUniversity of Texas Southwestern Medical Center
1 Previous Clinical Trials
30 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am fully active or can carry out light work.I have had treatments like radiotherapy, chemotherapy, or surgery for prostate cancer.My prostate cancer was confirmed by a biopsy within the last 18 months.I am older than 45 years.You cannot have the UroLift System placed if you have:I don't have urethral conditions that would prevent UroLift System procedures.I am currently on hormone therapy for cancer.My urinary symptoms are severe, with an AUA score of 17 or more.My prostate cancer is early stage, not spread, with specific Gleason scores.My PSA test was not done too close to certain prostate procedures or treatments.I agree to use effective birth control or abstain from sex during and for 90 days after the study.My prostate is smaller than 100 grams, as measured by ultrasound or MRI.My health is good to moderately impaired.I can be safely put under general anesthesia for less than an hour.I have urinary incontinence because of a weak bladder sphincter.I currently have a urinary tract infection.I have had surgery or procedures for an enlarged prostate.I do not have more than half of my biopsy samples showing cancer with specific risk factors.You are allergic to nickel, titanium, or stainless steel.
Research Study Groups:
This trial has the following groups:- Group 1: All Study participants
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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